Clinical Features of Clonal Cytogenetic Abnormalities in Philadelphia-negative Cells Developed During Tyrosine Kinase Inhibitor Treatment

被引:0
作者
Oiwa, Kana [1 ,2 ]
Lee, Shin [1 ,3 ]
Fujita, Kei [1 ,3 ]
Ueda, Takanori [1 ]
Yamauchi, Takahiro [1 ]
机构
[1] Univ Fukui, Div Hematol & Oncol, Fukui, Japan
[2] Osu Hosp, Div Internal Med, Nagoya, Japan
[3] Matsunami Gen Hosp, Dept Hematol, Kasamatsu, Japan
关键词
chromosomal abnormalities; tyrosine kinase inhibitor; monosomy; 7; trisomy; 8; secondary myelodysplastic syndrome/acute myeloid leukemia; CHRONIC MYELOID-LEUKEMIA; MYELODYSPLASTIC SYNDROME; JAPANESE PATIENTS; IMATINIB; MONOSOMY-7; ABL;
D O I
10.2169/internalmedicine.2182-23
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Most clonal cytogenetic abnormalities of Philadelphia -negative cells (CCA/Ph-) occurring during tyrosine kinase inhibitor (TKI) treatment are transient, and the development of secondary myelodysplastic syndrome (MDS)/acute myeloid leukemia (AML) is rare, but the frequency and clinical significance in Japanese patients are still unknown. We herein report four patients who developed CCA/Phduring TKI therapy and were diagnosed with secondary MDS/AML. The duration from TKI therapy initiation to MDS/AML onset ranged from 3 to 48 months, and the survival ranged from 5 to 84 months. The occurrence of CCA/Phwith MDS/AML may be associated with a poor prognosis, and careful follow-up is recommended for patients who receive TKI therapy.
引用
收藏
页码:729 / 732
页数:4
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